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FDA Inspection 791042 — Kem Medical Products Corp

Kem Medical Products Corp — FEI 2432141

The FDA completed an inspection of Kem Medical Products Corp on July 10, 2012 in Hauppauge, NY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 10, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Hauppauge, NY (United States)

Facility

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